Department of Histopathology, King Edward Memorial Hospital, Perth and School for Women's and Infants' Health, University of Western Australia, Perth, Western Australia, Australia (C.J.R.S).
Int J Gynecol Pathol. 2021 May 1;40(3):224-228. doi: 10.1097/PGP.0000000000000694.
A 30-yr-old patient with no significant past medical history presented with postcoital bleeding and was found to have fibrinous pseudomembranous lesions overlying and partly in continuity with the endocervical mucosa. Histologically, these were characterized by an atypical microglandular proliferation that was associated with extensive fibrinous exudate and a prominent neutrophil polymorph infiltrate. Ligneous stromal alteration was not identified but the changes prompted hematologic review which confirmed plasminogen deficiency. A subsequent endometrial biopsy also demonstrated degenerate glands within a fibrin-rich matrix. This is the third case demonstrating an association between atypical endocervical microglandular hyperplasia and plasminogen deficiency. The diagnosis should also be considered when biopsies demonstrate exuberant fibrin exudate even if ligneous disease is not present.
一位 30 岁的患者,无明显既往病史,出现性交后出血,发现宫颈黏膜表面覆盖有纤维素性假膜状病变,部分与宫颈内口黏膜相连。组织学上,这些病变的特征是不典型的微小腺体增生,伴有广泛的纤维素性渗出物和显著的中性粒细胞多形核浸润。未发现木样变间质改变,但这些改变促使进行血液学检查,结果证实存在纤溶酶原缺乏。随后的子宫内膜活检也显示在富含纤维蛋白的基质中有退化的腺体。这是第三个显示不典型宫颈微小腺体增生与纤溶酶原缺乏相关的病例。即使不存在木样变,当活检显示纤维蛋白样渗出物丰富时,也应考虑诊断。